ascorbic-acid and stannic-oxide

Pico sized Stannous oxide particles (SnO PPs) were synthesized in an ethanol-water solvent system on the surface of nitrogen doped graphene oxide (GO). The highly conductive support was a combination of dual interactions between 4-aminomethylbenzylamine (AMBA) and GO. The oppositely positioned -NH

Topics: Ascorbic Acid; Biosensing Techniques; Ethanol; Graphite; Limit of Detection; Oxides; Reproducibility of Results; Tin Compounds; Water

The green synthesis of tin oxide nanoparticles (SnO

Topics: Animals; Animals, Newborn; Antioxidants; Ascorbic Acid; Body Weight; Female; Green Chemistry Technology; Male; Metal Nanoparticles; Microscopy, Electron, Transmission; Rats, Sprague-Dawley; Spectroscopy, Fourier Transform Infrared; Tin Compounds

Three types of Zinc oxide (ZnO) nanostructures viz. ZnO nanocrystals (ZnONCs), ZnO nanoparticles (ZnONPs) and ZnO nanobelts (ZnONBs) were synthesized and characterized by UV-Vis, FTIR and SEM. A comparison of signal amplification by these ZnO nanostructures as judged by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and Linear Sweep Voltammetry (LSV) revealed that ZnONCs are better sensing interface for electrochemical detection. When these ZnO nanostructure were compared electrochemically for sensing Vitamin C, ZnONC's sensor outperformed the ZnONP and ZnONB sensor and previously reported sensors. The ZnONCs/MB/FTO electrode showed a wide linear sensing range (0.001μM to 4000μM), low detection limit (0.0001μM), a small response time (5s) and a storage stability of 6months. To the best of our knowledge, this elevated sensitivity and remarkable stability for electrochemical Vitamin C detection using ZnONC's have not been reported so far.

Topics: Ascorbic Acid; Beverages; Calibration; Dielectric Spectroscopy; Electrochemical Techniques; Electrodes; Fluorine; Glass; Limit of Detection; Spectrophotometry, Ultraviolet; Spectroscopy, Fourier Transform Infrared; Tin Compounds; X-Ray Diffraction; Zinc Oxide

A three-dimensional (3D) continuous and interconnected network graphene foam (GF) was synthesized by chemical vapor deposition using nickel foam as a template. The morphologies of the GF were observed by scanning electron microscopy. X-ray diffraction and Raman spectroscopy were used to investigate the structure of GF. The graphene with few layers and defect free was closely coated on the backbone of the 3D nickel foam. After etching nickel, the GF was transferred onto indium tin oxide (ITO) glass, which acted as an electrode to detect uric acid using cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The GF/ITO electrode showed a high sensitivity for the detection of uric acid: approximately 9.44 mA mM(-1) in the range of 25 nM-0.1 μM and 1.85 mA mM(-1) in the range of 0.1-60 μM. The limit of detection of GF/ITO electrode for uric acid is 3 nM. The GF/ITO electrode also showed a high selectivity for the detection of uric acid in the presence of ascorbic acid. This electrode will have a wide range of potential application prospects in electrochemical detection.

Topics: Antioxidants; Ascorbic Acid; Biosensing Techniques; China; Electrochemical Techniques; Electrodes; Graphite; Humans; Imaging, Three-Dimensional; Indium; Limit of Detection; Microscopy, Electron, Scanning; Spectrum Analysis, Raman; Tin Compounds; Uric Acid; X-Ray Diffraction

Developing new tools and technologies to enable recording the dynamic changes of multiple neurochemicals is the essence of better understanding of the molecular basis of brain functions. This study demonstrates a microfluidic chip-based online electrochemical system (OECS) for in vivo continuous and simultaneous monitoring of glucose, lactate, and ascorbate in rat brain. To fabricate the microfluidic chip-based detecting system, a microfluidic chip with patterned channel is developed into an electrochemical flow cell by incorporating the chip with three surface-modified indium-tin oxide (ITO) electrodes as working electrodes, a Ag/AgCl wire as reference electrode, and a stainless steel tube as counter electrode. Selective detection of ascorbate is achieved by the use of single-walled carbon nanotubes (SWNTs) to largely facilitate the electrochemical oxidation of ascorbate, while a dehydrogenase-based biosensing mechanism with methylene green (MG) adsorbed onto SWNTs as an electrocatalyst for the oxidation of dihydronicotiamide adenine dinucleotide (NADH) is employed for biosensing of glucose and lactate. To avoid the crosstalk among three sensors, the sensor alignment is carefully designed with the SWNT-modified electrode in the upstream channel and paralleled glucose and lactate biosensors in the downstream channels. With the microfluidic chip-based electrochemical flow cell as the detector, an OECS is successfully established by directly integrating the microfluidic chip-based electrochemical flow cell with in vivo microdialysis. The OECS exhibits a good linear response toward glucose, lactate, and ascorbate with less crosstalk. This property, along with the high stability and selectivity, enables the OECS for continuously monitoring three species in rat brain following brain ischemia.

Topics: Animals; Ascorbic Acid; Biosensing Techniques; Brain Chemistry; Brain Ischemia; Electrochemistry; Electrodes; Glucose; Indicators and Reagents; Indium; Lactic Acid; Male; Microcomputers; Microfluidic Analytical Techniques; Oxidation-Reduction; Rats; Rats, Sprague-Dawley; Reproducibility of Results; Tin Compounds

In this paper, a simple and sensitive sandwich-type photoelectrochemical (PEC) immunosensor for measurement of biomarkers on a gold nanoparticle-modified indium tin oxide (ITO) electrode through electrodeposition for point-of-care testing was developed by using a tin dioxide quantum dot-graphene nanocomposite (G-SnO2) as an excellent label with amplification techniques. The capture antibody (Ab1) was firstly immobilized on the gold nanoparticle-modified ITO electrode due to the covalent conjugation, then the antigen and the AuNP/PDDA-G-SnO2 nanocomposite nanoparticle labeled signal antibody (Ab2) were conjugated successively to form a sandwich-type immunocomplex through a specific interaction. Under irradiation with a common ultraviolet lamp (∼365 nm, price $50), the SnO2 NPs were excited and underwent charge-separation to yield electrons (e(-)) and holes (h(+)). As the holes were scavenged by ascorbic acid (AA), the electrons were transferred to the ITO electrode through RGO to generate a photocurrent. The photocurrents were proportional to the CEA concentrations, and the linear range of the developed immunosensor was from 0.005 to 10 ng mL(-1) with a detection limit of 0.036 pg mL(-1). The proposed sensor shows high sensitivity, stability, reproducibility, and can become a promising platform for other biomolecular detection.

Topics: Ascorbic Acid; Electrochemical Techniques; Gold; Graphite; Light; Metal Nanoparticles; Microscopy, Electron, Transmission; Neoplasms; Photochemical Processes; Quantum Dots; Tin Compounds; Ultraviolet Rays

With the objective of producing a material showing better conductive properties to be used as a support for electroactive species, a SiO(2)/SnO(2) mixed oxide was prepared. The procedure for SiO(2)/SnO(2) mixed oxide preparation using the sol-gel processing method, starting from tetraethylorthosilicate and SnI(4) as precursor reagents, is described. SiO(2)/SnO(2) with composition Sn=15.6 wt% and S(BET) = 525 m(2)g(-1), V(p)=0.28 mlg(-1), and D(p)= 1.5 nm, where S(BET), V(p) and D(p) are the specific surface area, the average pore volume, and the average pore diameter, respectively, was obtained. The X-ray photoelectron spectroscopy showed that the mixed oxide was thermally very stable for samples heat-treated at up to 1073 K. The Brønsted acid sites, probed with pyridine molecules for samples heat-treated at various temperatures, were chemically stable up to 473 K. Segregation of SnO(2) crystalline phase was observed at 1473 K but no crystalline phase was verified for SiO(2) at this temperature. The porous SiO(2)/SnO(2) matrix was used as base for Cu(II) immobilization and an electrode was developed for application in electrochemical detection of vitamin C in tablets.

Topics: Ascorbic Acid; Copper; Electrochemistry; Electron Probe Microanalysis; Hot Temperature; Models, Chemical; Phase Transition; Silanes; Silicon Dioxide; Thermogravimetry; Time Factors; Tin Compounds; X-Ray Diffraction